1. Latest News
  2. Submit Press Release
  1. PR Home
  2. Latest News
  3. Feeds
  4. Alerts
  5. Submit Free Press Release
  6. Journalist Account
  7. PRNewswire Distribution

Live Webinar-Applying GMP Quality Principles To Establish A Reduced Testing Program

Who will benefit: Quality Control Laboratory Manager Warehousing Purchasing Managers Procurement Managers Laboratory Analyst Cost Accounting

 
PRLog - Jul. 18, 2011 - Summary
This webinar will discuss current regulatory and quality requirements for reduced testing of components used in pharmaceuticals and medical devices. Reduced testing will be viewed from current industry practice, the regulations, and quality principles. The reduced testing lifecycle we studied and reviewed. This includes such topics as component specifications, material qualification, supplier auditing and qualification, collaborative laboratory testing, certificates of analysis, material validation sampling, analyzing testing, qualification, and disqualification. Examples of systems will be shown. This webinar will primarily use graphics, especially flowcharts, to demonstrate the principles and increase in understanding of the topics.

Details


Discount : Get 15 % Discount as a early bird registrations. Use Promo code CGO15

Reduced testing test permits a medical product manufacturer to reduce testing of incoming components provided there are adequate controls on specification control, material qualification, supplier qualification & monitoring, material validation, and collaborative testing. Industry practice in the performance of reduced testing has resulted in new and modified expectations and requirements.

The benefits of systematic reduced testing program include increased compliance, smaller inventory cycles, less testing, less handling, and increased productivity and efficiency.

As industry has been looking to reduce costs, improve efficiency, the FDA has begun to more closely scrutinize the industry’s effort to make certain that the above mentioned controls are in place. In this effort the FDA is focusing on supplier control and sampling issues.
Why should you attend :

Reasons for attending this webinar include the following:
To understand the compliance and quality requirements for reducing incoming material testing on pharmaceutical and medical device components.
To gain knowledge applicable to  the control and qualification of suppliers that will increase compliance and improve efficiency
To reduce costs and increase efficiency in the handling of incoming materials and components.

Areas Covered in the Session:

Advantages and disadvantages of reduced testing
Basic review of quality systems.
Brief review of regulatory requirements.
Differences between suppliers and contractors.
Interdepartmental roles in establishing and maintaining a reduced testing program.
A study of the reduced testing lifecycle in graphical format , including specification control, material qualification, researching and selecting suppliers, supplier auditing (including selection of audit team members) and qualification, corrective actions, handling certificates of analysis, maintaining supplier quality and control, supplier change control, and handling problems suppliers.
Logistics of implementing a reduced testing plan

Who will benefit:

Quality Control
Laboratory Manager
Warehousing Purchasing Managers
Procurement Managers
Laboratory Analyst
Cost Accounting

About the speaker:

Howard enjoys sharing his 30 years plus experience in starting up, developing, implementing, managing, and remediating pharmaceutical and medical device quality systems. One of his favorite areas is material and supplier control from which he receives great satisfaction in applying his knowledge for improvement.                                                                      
He has a BS in Biology/Chemistry and Political Science as well as work toward an MBA. His ability to quickly learn the technology is demonstrated by his success in applying quality assurance principles to a wide range of pharmaceuticals and medical devices. He is a Certified Biomedical Auditor (CBA), Certified Quality Manager (CQM), and Quality Auditor (CQA). His technical education is further complemented by his Political Science degree helping him understand the regulatory process; his work toward an MBA provides business insight. He is a member of ASQ, PDA, AAMI, RAPS, and SQA.                                                                                                                                                        
He strongly believes that Quality is very influential in shaping successful operations. He knows how to use his leadership abilities to build organizational relationships that make systems operate effectively as well as to develop and empower people.

For any assistance contact us at support@compliance2go.com or call us at 877.782.4696

--- End ---

Click to Share

Contact Email:
***@compliance2go.com Email Verified
Source:Compliance2go.com
Country:United States
Industry:Biotech, Medical, Health
Tags:Online Compliance Training, webcast, compliance training, gmp, life science, medical device, biotechnology, fda, Pharmace
Shortcut:prlog.org/11589493
Disclaimer:   Issuers of the press releases are solely responsible for the content of their press releases. PRLog can't be held liable for the content posted by others.   Report Abuse

Latest Press Releases By “

More...

Trending News...



  1. SiteMap
  2. Privacy Policy
  3. Terms of Service
  4. Copyright Notice
  5. About
  6. Advertise
Like PRLog?
9K2K1K
Click to Share